Clinical Research Coordinator

Overview

• Coordinate clinical trials, ensuring adherence to protocols, ethical standards, and regulatory guidelines while contributing to impactful research outcomes.
• Collaborate with multidisciplinary teams to manage research studies and optimize participant engagement and retention.
• Oversee data collection, analysis, and documentation to maintain accuracy and integrity in research records.
• Ensure logistical readiness by managing equipment, supplies, and site-specific requirements effectively.
• Provide oversight for multiple trials, monitoring participant health and adherence to study protocols.
• Offer opportunities for professional growth through training and skill development in clinical research practices.
• Contribute to advancing healthcare research, particularly in oncology, within a dynamic and supportive environment.

Key Responsibilities & Duties

• Monitor and manage clinical trials, ensuring compliance with study protocols and regulatory requirements.
• Collect, analyze, and maintain accurate research data and documentation.
• Engage with study participants, conducting interviews and ensuring adherence to study guidelines.
• Coordinate with laboratories and regulatory bodies to maintain compliance and quality standards.
• Manage specimen collection, labeling, and transportation in accordance with established protocols.
• Recruit, screen, enroll, and randomize study participants, ensuring a smooth onboarding process.
• Address protocol deviations and resolve queries related to electronic data capture systems.
• Support administrative tasks, including stipend payments and trial documentation management.

Job Requirements

• Associate of Science degree in a health-related field; Bachelor's degree preferred.
• Minimum of 2 years of clinical research experience; oncology experience highly desirable.
• Proficiency in regulatory filing, study submission, and compliance monitoring.
• Strong interpersonal skills for participant interaction, including informed consent and medical history collection.
• Experience in phlebotomy, vital signs monitoring, and ECG administration is advantageous.
• Ability to manage administrative tasks and stipend payments efficiently.
• Willingness to work on-site full-time and travel between designated locations as required.
• Excellent organizational and communication skills to manage multiple trials simultaneously.